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Merck

454710

Sigma-Aldrich

聚三氟氯乙烯

powder

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About This Item

线性分子式:
[CF2CF(Cl)]n
CAS号:
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

形狀

powder

介電常數

2.6, 1 kHz (ASTM D 150)

硬度

75-85 (Shore D)

參數

2E-3 cc/sec flow rate (230°C 100 MPa)

轉變溫度

Tg (DSC) 103 °C (onset)
Tm (DSC) 210 °C (onset)

密度

1 g/mL at 25 °C

SMILES 字串

F\C(F)=C(/F)Cl

InChI

1S/C2ClF3/c3-1(4)2(5)6

InChI 密鑰

UUAGAQFQZIEFAH-UHFFFAOYSA-N

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應用

阀、密封材料、包装薄膜、电荧发光显示板、需要具有耐磨损特性的轴承。

特點和優勢

耐化学性、几乎完全不吸湿的特性、低蠕变、高透光性、高电绝缘性能、不易燃且热膨胀系数低。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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R J Greene et al.
Journal of analytical toxicology, 16(1), 28-32 (1992-01-01)
3.1 Oil, referred to as polychlorotrifluoroethylene (pCTFE), is a polymeric mixture consisting primarily of trimers and tetramers of chlorotrifluoroethylene (CTFE) end-capped with chlorine. Inhalation studies have associated dose-related body weight loss, increased organ weights, and abnormal hepatic enzyme activities with
C E Jones et al.
Journal of applied toxicology : JAT, 11(1), 51-60 (1991-02-01)
Polychlorotrifluoroethylene (polyCTFE--primarily oligomers with 3-4 monomer units), a non-flammable hydraulic fluid for aircraft, was given daily for 15 days by oral gavage to four Rhesus monkeys at a concentration of 0.725 g kg-1. The administered dose was at a level
S Saneinejad et al.
Journal of biomedical materials research, 50(4), 465-474 (2000-04-11)
Central nervous system (CNS) neurons, unlike those of the peripheral nervous system, do not spontaneously regenerate following injury. Recently it has been shown that in the developing CNS, a combination of cell-adhesive and cell-repulsive cues guide growing axons to their
Studies on the toxicity of pyrolytic products of polychlorotrifluoroethylene.
T Hirota
Bulletin of the Osaka Medical College, 34(1-2), 27-36 (1988-11-01)
E R Kinkead et al.
Toxicology and industrial health, 7(4), 295-307 (1991-07-01)
C8 polychlorotrifluoroethylene (pCTFE) oligomers accumulate preferentially in the liver during long-term oral exposure and appear to be more hepatotoxic than C6 oligomers. A repeated-dose gavage study was initiated to determine the relative contributions of the corresponding C6 (trimer) and C8

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